Safety assessment of propyl-propane-thiosulfonate (PTSO): 90-days oral subchronic toxicity study in rats
Propyl-propane-thiosulfonate (PTSO) is one of the main organosulfur compounds present in Allium essentials oil. Different applications in the food sector have been proposed for PTSO, such as food and feed additive and as active packaging. However, the authorization of its use depends on its toxicity...
| Autores: | , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2020 |
| País: | España |
| Institución: | Universidad de Sevilla (US) |
| Repositorio: | idUS. Depósito de Investigación de la Universidad de Sevilla |
| OAI Identifier: | oai:idus.us.es:11441/128501 |
| Acceso en línea: | https://hdl.handle.net/11441/128501 https://doi.org/10.1016/j.fct.2020.111612 |
| Access Level: | acceso abierto |
| Palabra clave: | Subchronic toxicity 90-day Organosulfur compounds Allium Propyl-propanethiosulfonate |
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Safety assessment of propyl-propane-thiosulfonate (PTSO): 90-days oral subchronic toxicity study in ratsCascajosa Lira, AntonioPrieto Ortega, Ana IsabelBaños, AlbertoGuillamón, EnriqueMoyano, RosarioJos Gallego, Ángeles MencíaCameán Fernández, Ana MaríaSubchronic toxicity90-dayOrganosulfur compoundsAlliumPropyl-propanethiosulfonatePropyl-propane-thiosulfonate (PTSO) is one of the main organosulfur compounds present in Allium essentials oil. Different applications in the food sector have been proposed for PTSO, such as food and feed additive and as active packaging. However, the authorization of its use depends on its toxicity profile. Thus, as a part of its safety assessment, in this work a repeated dose 90-day oral toxicity study has been conducted for the first time in rats following the OECD guideline 408. PTSO was administered to groups of 10 male and 10 female rats at dose levels of 0, 14, 28, and 55 mg/kg/day. No clinical signs or mortality and no changes in body weight, food consumption and feed conversion efficiency were detected through the study. Moreover, no treatment-related changes in hematological and biochemical parameters were observed, for either sex or dose groups. The histopathology study performed revealed no differences in organ weights, and no morphological and histopathological changes were observed. Based on these results, the no-observed-adverse-effect level (NOAEL) of PTSO was judged to be ≥ 55 mg/kg/day for both sexes.Ministerio de Ciencia e Innovación (Project RTC-2017-6199-2)Junta de Andalucía (Project AT 2017-5323)ElsevierNutrición y Bromatología, Toxicología y Medicina LegalMinisterio de Ciencia e Innovación (MICIN). EspañaJunta de Andalucía2020info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionapplication/pdfapplication/pdfhttps://hdl.handle.net/11441/128501https://doi.org/10.1016/j.fct.2020.111612reponame:idUS. Depósito de Investigación de la Universidad de Sevillainstname:Universidad de Sevilla (US)InglésFood and Chemical Toxicology, 144, 111612.RTC-2017-6199-2AT 2017-5323https://doi.org/10.1016/j.fct.2020.111612info:eu-repo/semantics/openAccessoai:idus.us.es:11441/1285012026-06-17T12:51:07Z |
| dc.title.none.fl_str_mv |
Safety assessment of propyl-propane-thiosulfonate (PTSO): 90-days oral subchronic toxicity study in rats |
| title |
Safety assessment of propyl-propane-thiosulfonate (PTSO): 90-days oral subchronic toxicity study in rats |
| spellingShingle |
Safety assessment of propyl-propane-thiosulfonate (PTSO): 90-days oral subchronic toxicity study in rats Cascajosa Lira, Antonio Subchronic toxicity 90-day Organosulfur compounds Allium Propyl-propanethiosulfonate |
| title_short |
Safety assessment of propyl-propane-thiosulfonate (PTSO): 90-days oral subchronic toxicity study in rats |
| title_full |
Safety assessment of propyl-propane-thiosulfonate (PTSO): 90-days oral subchronic toxicity study in rats |
| title_fullStr |
Safety assessment of propyl-propane-thiosulfonate (PTSO): 90-days oral subchronic toxicity study in rats |
| title_full_unstemmed |
Safety assessment of propyl-propane-thiosulfonate (PTSO): 90-days oral subchronic toxicity study in rats |
| title_sort |
Safety assessment of propyl-propane-thiosulfonate (PTSO): 90-days oral subchronic toxicity study in rats |
| dc.creator.none.fl_str_mv |
Cascajosa Lira, Antonio Prieto Ortega, Ana Isabel Baños, Alberto Guillamón, Enrique Moyano, Rosario Jos Gallego, Ángeles Mencía Cameán Fernández, Ana María |
| author |
Cascajosa Lira, Antonio |
| author_facet |
Cascajosa Lira, Antonio Prieto Ortega, Ana Isabel Baños, Alberto Guillamón, Enrique Moyano, Rosario Jos Gallego, Ángeles Mencía Cameán Fernández, Ana María |
| author_role |
author |
| author2 |
Prieto Ortega, Ana Isabel Baños, Alberto Guillamón, Enrique Moyano, Rosario Jos Gallego, Ángeles Mencía Cameán Fernández, Ana María |
| author2_role |
author author author author author author |
| dc.contributor.none.fl_str_mv |
Nutrición y Bromatología, Toxicología y Medicina Legal Ministerio de Ciencia e Innovación (MICIN). España Junta de Andalucía |
| dc.subject.none.fl_str_mv |
Subchronic toxicity 90-day Organosulfur compounds Allium Propyl-propanethiosulfonate |
| topic |
Subchronic toxicity 90-day Organosulfur compounds Allium Propyl-propanethiosulfonate |
| description |
Propyl-propane-thiosulfonate (PTSO) is one of the main organosulfur compounds present in Allium essentials oil. Different applications in the food sector have been proposed for PTSO, such as food and feed additive and as active packaging. However, the authorization of its use depends on its toxicity profile. Thus, as a part of its safety assessment, in this work a repeated dose 90-day oral toxicity study has been conducted for the first time in rats following the OECD guideline 408. PTSO was administered to groups of 10 male and 10 female rats at dose levels of 0, 14, 28, and 55 mg/kg/day. No clinical signs or mortality and no changes in body weight, food consumption and feed conversion efficiency were detected through the study. Moreover, no treatment-related changes in hematological and biochemical parameters were observed, for either sex or dose groups. The histopathology study performed revealed no differences in organ weights, and no morphological and histopathological changes were observed. Based on these results, the no-observed-adverse-effect level (NOAEL) of PTSO was judged to be ≥ 55 mg/kg/day for both sexes. |
| publishDate |
2020 |
| dc.date.none.fl_str_mv |
2020 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion |
| format |
article |
| status_str |
acceptedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/11441/128501 https://doi.org/10.1016/j.fct.2020.111612 |
| url |
https://hdl.handle.net/11441/128501 https://doi.org/10.1016/j.fct.2020.111612 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Food and Chemical Toxicology, 144, 111612. RTC-2017-6199-2 AT 2017-5323 https://doi.org/10.1016/j.fct.2020.111612 |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf application/pdf |
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Elsevier |
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Elsevier |
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reponame:idUS. Depósito de Investigación de la Universidad de Sevilla instname:Universidad de Sevilla (US) |
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Universidad de Sevilla (US) |
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idUS. Depósito de Investigación de la Universidad de Sevilla |
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idUS. Depósito de Investigación de la Universidad de Sevilla |
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15.300724 |